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Access through your institution Buy or subscribe Most retroviral vectors used for gene therapy are derived from C-type viruses, which cannot infect quiescent cells. Lentiviruses such as
HIV-1, on the other hand, can infect quiescent cells, but concerns have been raised about their safety for human gene therapy. In this issue, Parveen et al. (see p. 623) describe how they
developed an engineered retroviral vector that has the safety features of spleen necrosis virus (SNV), a C-type retroviral vector, and that can efficiently infect quiescent cells. Previous
studies have suggested that HIV-1 can infect nondividing cells with the help of a nuclear localization sequence (NLS) located in the matrix protein. The matrix proteins of SNV and HIV-1 are
structurally similar, so the researchers tried mutating residues in the region of the SNV matrix protein analogous to the NLS in HIV-1. They found that by altering just two amino acids, they
could produce a C-type retroviral vector capable of infecting growth-arrested human T lymphocytes and quiescent primary monocyte-derived macrophages. In addition to its implications for
gene therapy, the results support the notion that the NLS is sufficient to mediate the ability of HIV-1 to infect nondividing cells. This is a preview of subscription content, access via
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* Learn about institutional subscriptions * Read our FAQs * Contact customer support Authors * Meeghan Sinclair View author publications You can also search for this author inPubMed Google
Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Sinclair, M. Retroviral vector for quiescent cells?. _Nat Biotechnol_ 18, 587 (2000).
https://doi.org/10.1038/76399 Download citation * Issue Date: June 2000 * DOI: https://doi.org/10.1038/76399 SHARE THIS ARTICLE Anyone you share the following link with will be able to read
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